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MANAGEMENT OF DIABETIC FOOT INFECTIONS & OSTEOMYELITIS
DR. P.C. CHYE Consultant Orthopaedic Surgeon Dept. Orthopaedic Surgery & Traumatology Hospital Kuala Lumpur
DIABETES MELLITUS
Global Prevalence :
2003 : 194 million
2010 : 252 million
2025 : 380 million
PREVALENCE OF DM IN MALAYSIA (Population >30 years)
0.65%
2.10%
6.30%
8.30%
14.90%
1960 1982 1986 1996 2006
Year
Prevalence of Diabetes Mellitus in Malaysia
Prevalence
3rd National Health and Mortality &
Morbidity Survey
22%
08
DIABETIC FOOT INFECTIONS RISK FACTORS
HOST DEFENSE : Neutrophil functions : chemotaxis,phagocytosis, intracellular killing Monocyte & complement functions PERIPHERAL VASCULAR DISEASES : in blood supply needed to heal ulcers and infection SENSORY NEUROPATHY : in appreciation of pain and temperature injuries not noticed, severity underestimated MOTOR NEUROPATHY : anatomical foot deformity abnormal pressure points
ulceration AUTONOMIC NEUROPATHY : sweating, dry & cracked skin portal of bacteria entry
DIABETIC FOOT INFECTIONS - SPECTRUM
Ranges from cellulitis to infected ulcers, abscess, osteomyelitis , wet gangrenes and necrotising fasciitis
40% Mild 30-40% Moderate 20-30% Severe
40-80% Infected
(or suspected)
15-25% Develop Foot Ulcer
7% of Population
Diabetic
49% of diabetic patients with diabetic foot infection will develop infection in the other foot in 18 months
DIABETIC FOOT INFECTIONS THE DEVELOPMENT
Usually precipitated by trauma
Infection may start superficially in an ulcer or crack of the skin but can rapidly progress to involve deeper structures including tendons and bones
The anatomical structures of various compartments of the foot, tendon sheaths, ligaments, fascia and neurovascular bundles tends to facilitate proximal spread of the infection
Inflammation and infection in the foot compartments can cause compartment syndrome vascular thrombosis
DIABETIC FOOT INFECTIONS - PRESENTATIONS
Redness, swelling, discharging sinus/ulcer, gangrene, pain
Diabetic patient may or may not mount a fever, even in the presence of severe infection
50% of patients with a limb-threatening infection do not manifest systemic signs or symptoms leading to underestimation of the presence and severity of infection
The signs and symptoms are masked by neuropathy
Hypotension, tachycardia and severe unexplained hyperglycaemia are however often noted
DIABETIC FOOT INFECTIONS - PROGRESSION
Coexisting metabolic derangements, peripheral arterial disease, poor immune response poor delivery of antibiotics to the infected tissues, reduced access & functions of phagocytic cells to the infected area rapid progression of infection in hours or days & quickly become limb- or life-threatening
DIABETIC FOOT INFECTIONS
These wounds are usually more severe & more complicated to treat than do equivalent infections in persons without diabetes
DIABETIC FOOT INFECTIONS - BACTERIA INVOLVED
Aerobic Gram +ve cocci, esp (Staphylococcus aureus) are the predominant pathogens
In chronic ulcers or in patients who have recently received antibiotic therapy may be infected with Gram ve rods
In those with foot ischaemia and gangrene may have obligate anaerobic organisms
- Staphylococcus aureus 45%
- Streptococcus sp. 35%
- Enterococcus sp. 29%
- Staphylococcus epidermidis 23%
- Proteus mirabilis 26%
- Pseudomonas aeruginosa 16%
- Peptostreptococcus sp. 22%
- Diphtheroids 19%
- Bacteroides sp. 16%
Gram positive cocci
Microbial complexity
Microbial burden
Clinical risk
1 2 3 4
Anaerobes
Aerobic Gram-negative rods
Prior Rx
Necrosis
Depth
Severity
Limb-threatening infections are often polymicrobial
MULTIRESISTANT BACTERIAL INFECTIONS
Diabet Met 2004 Jul;21(7) : 710-5
Diabetic foot ulcer and multidrug-resistant
organisms: risk factors and impact. Hartemann-Heurtier A, Robert J, Jacqueminet S, Ha Van G, Golmard JL, Jarlier V, Grimaldi A.
Detected in 1/3 of patients with
previous history of hospital
admission for the same wound
Detected in 25% of patients
with osteomyelitis
ALMOST 50% of Staph aureus isolated are MRSA !
Clinical Microbiology & Infection- October 2005
Prevalence of methicillin-resistant Staphylococcus aureus in infected and uninfected diabetic foot ulcers
TIMELINE OF STAPHYLOCOCCAL RESISTANCE
1940 1950 1960 1970 1980 1990 2000 2010
Penicillin-resistance
GISA
CA-MRSA
VRSA
Sporadic MRSA Epidemic MRSA
DIABETIC FOOT INFECTIONS TREATMENT STRTEGIES
Require attention to both local & systemic issues
DIABETIC FOOT INFECTIONS -COMPREHENSIVE MANAGEMENT
TREAT THE ULCER & INFECTION, GET THE WOUND TO HEAL, PREVENT RECURRENCE
TREAT THE DIABETES, ASSOCIATED SYSTEMIC PROBLEMS & OVERCOME THE UNDERLYING PATHOLOGY
LOC
AL
ISSU
ES
SYST
EMIC
ISSU
ES
+
AT THE SAME TIME
DIABETIC FOOT INFECTIONS - MULTIDISCIPLINARY TEAM APPROACH
Comprehensive management of these patients requires care of a finely-tuned multidisciplinary team for medical stabilization, surgical debridement, antibiotic selection, vascular reperfusion, wound care, podiatric care, orthotic care, nutrition support, rehabilitation and delayed reconstruction to achieve functional limb salvage
EVALUATION AT 3 LEVELS
1 The patient as a whole 2 The affected limb or foot 3 The infected wound To determine : - presence, type, extent and severity of infection - pathogens involved - presence of any systemic consequences of infection - contribution of vascular disease / neuropathy - altered foot biomechanics that contributes to the cause of the wound ( and thus, its ability to heal )
DIABETIC FOOT INFECTIONS - INITIAL ASSESSMENT AND INVESTIGATIONS
BLOOD INVESTIGATIONS : - Full blood count - Erythrocyte Sedimentation Rate (ESR) - C- Reactive Protein (CRP) - Random / Fasting Sugar Levels - Glycosylated Haemoglobin - Renal Profile - Serum Albumin
DIABETIC FOOT INFECTIONS - INITIAL ASSESSMENT AND INVESTIGATIONS
EXAMINE THE FOOT : - Palpation/probing for fluctuance & tunneling wounds/ ulcer (deep
infection) - a clinically infected ulceration probes to bone 89-95% osteomyelitis - Blood supply : Dorsalis Pedis , Posterior Tibialis & Popliteal pulses.
Ankle-Brachial Systolic Index ( ABSI ), Doppler, Evidence of ischaemia & gangrene
- the degree of impaired limb perfusion significantly reduce the chances of wound healing, increases the overall severity of infection and risk of amputations
- Sensation --- Neuropathy pain in an insensate foot means severe infection
- Deformities & Abnormal Pressure Points
DIABETIC FOOT INFECTIONS - INITIAL ASSESSMENT AND INVESTIGATIONS
TAKE AN X-ray : - Osteomyelitis - Gas Gangrene - Presence of Foreign Body - Osseous deformities / fractures / dislocations MRI is more sensitive and specific, especially for extent of soft tissue involvement
DIABETIC FOOT INFECTIONS INITIAL MANAGEMENT
IDENTIFY THE ORGANISMS INVOLVED : - Send appropriately obtained speciments for culture before
starting empirical antibiotic therapy - Soft tissue or bone speciments obtained by biopsy, curettage, or
aspiration are preferable - Superficial swab cultures of infected ulcers often complicate
evaluation of the infection - Definitive antibiotic therapy will be based on C&S results from intra-op cultures
Initial treatment in a previously untreated patient with a non-limb-threatening infection is focused on Staphylococcus and Streptococcus sp
Initial treatment of limb-threatening infections requires broad-spectrum antibiotics covering Staph aureus, group B Streps, other Streptococcus sp., enterobacteriaceae & anaerobes
DIABETIC FOOT INFECTIONS INITIAL MANAGEMENT ANTIBIOTIC SELECTION
Characteristic odours or history of resistant bacterial infections affect initial antibiotic choices
Antibiotic vary in how well they achieve effective concentration in the infected diabetic foot -- affected by the arterial blood supply to the foot & pharmacodynamic properties of the drug
DIABETIC FOOT INFECTIONS INITIAL MEDICAL MANAGEMENT
The degree of end organ dysfunction affects multiple aspects of medical and surgical management
Antibiotic dosing adjustment issues, poor cardiac function, hyperglycaemia, ketoacidosis, dehydration, hyperosmolality, electrolyte imbalance, renal insufficiency, anaemia, poor limb perfusion, immunosuppression, poor nutrition, poor healing potential often coexist
The goal of medical management is to regulate and normalize the metabolic and haemodynamic derangements and to prevent further decompensations
STABILIZE / RESUSCITATE THE PATIENT
Restore fluid and electrolyte balances, correct anemia, hyperglycaemia,
hyperosmolarity, acidosis &
treat other exacerbating
disorders
Optimize treatment of other
medical illnesses : ischaemic
heart disease, heart failure,
renal impairment etc
May need resuscitation
eg sepsis, ketoacidosis
DETERMINE THE NEED FOR SURGERY
When a non-healing infected diabetic foot ulcer is worsening despite adequate wound care and cultured-directed antibiotics, urgent surgery is needed
Emergency surgical intervention :
Life- or limb-threatening infection
eg. Necrotising fasciitis
Gas gangrene
Critical limb ischaemia
Deep abscess
OVERVIEW OF SURGICAL MANAGEMENT OF INFECTED DIABETIC FOOT
To achieve a healed wound & prevent
major amputation of the leg :
Darinage of pus, remove necrotic soft
tissue & bone + creating a healthy
wound bed
Limb reperfusion
Soft Tissue Cover
Correct deformity, relieve pressure areas
Restore stability, alignment & function
Reduce risk of reulceration & subsequent amputation
SUCCESSFUL SALVAGE
Incision & drainage Debridement Sequestrectomy Disarticulation Ray Amputation
DIABETIC FOOT INFECTIONS INITIAL SURGICAL DEBRIDEMENT
After patient is medically stabilised
Must be timely and aggressive Remove all sloughs, necrotic and marginal-looking tissues, dead bones, drain all pus, explore all sinus tracts Exposed tendons should be excised if proximal migration of infection is suspected
Exploration is done to determine involvement of fascial planes
The degree of intra-operative bleeding must be assessed Aims to reduce the bacterial load in the wound, create a healthy environment
to restore the physiologic processes of tissue repair and healing
Changes stubborn non-healing chronic wounds into acute wounds
Deep tissue & bone : C&S HPE ( if osteomyelitis suspected)
Crucial to successful control of infection and must be done as soon as possible
In severe infections, general anaesthesia is often needed as the depth of infection and fascial spread may be extensive
ANTIBIOTICS THERAPY
OFTEN INSUFFICIENT WITHOUT APPROPRIATE WOUND CARE
TREAT THE INFECTION, DO NOT STERILISE THE WOUND
Based on culture & sensitivity results, depth and severity of infection CONTINUED UNTIL RESOLUTION OF INFECTION, NOT UNTIL THE WOUND HAS HEALED
DIABETIC FOOT INFECTIONS --- WOUND BED PREPARATION
Converting a chronic wound into a wound with the potential to heal
Involves debridement, control of infection and inflammation, moisture control, excision of wound edges and callus
"TIME - "T" refers to the need to remove necrotic and diseased Tissue - "I" indicates the need to control bacterial burden and Infection - "M" refers to restoration of Moisture balance - "E" stands for the healing Edge, which is the point at which the wound is optimally primed for healing
DIABETIC FOOT INFECTIONS --REPEATED SHARP DEBRIDEMENT
Repeated sharp debridement is done until all necrotic tissues and bone + biofilms are removed
Stimulates production of growth factors and proliferation of collagen and fibroblasts
A healthy wound bed is created for granulation tissue to grow and wound to heal
REPEATED DEBRIDEMENT - ULTRASONIC DEBRIDEMENT
Use of low frequency cavitational ultrasound to debride away dead tissues, leaving healthy and granulation tissue intact
Also removes bacteria and biofilms
Sterile saline solution transfer the ultrasonic energy to the wound where tiny vibrating gas bubbles and cellular level fluid movement separates dead from healthy tissues
Safe, cost effective , painless alternative to painful sharp debridements
Low-frequency ultrasound has been shown to have cellular-level physical effects, known as cavitation and microstreaming, that can promote healing
Cavitation is the formation and oscillation of microscopic bubbles, which expand and collapse as they resonate with the ultrasound frequency
Acoustic microstreaming is the physical force of sound pressure waves that can displace small molecules and move fluids along and/or through cell membranes.
REPEATED DEBRIDEMENT - HYDROSURGICAL DEBRIDEMENT
Versajet Hydrosurgery System ( Smith & Nephew) - utilises a high-pressure jet of sterile saline that travels
parallel to the wound surface
- This high-speed jet creates a Venturi effect that enables the surgeon to simultaneously hold, cut and remove tissue, while irrigating and aspirating the wound, with a single instrument
Enables rapid debridement, likely to result in shorter procedure times
Clean wounds potentially reduce the number of required debridement procedures
Single device technique - combining lavage and sharp debridement instrumentation
Multiple tip configurations enhance procedural flexibility
REPEATED DEBRIDEMENT - Maggots Debridement Therapy
Sterile larva of the greenbottle fly is applied to the wound for 2-3 days
Necrotic tissues are eaten away
In late 1920s, William Baer from Johns Hopkins University, used maggots to treat children with osteomyelitis and soft tissue infections
Successfully performed by thousands of physicians throughout 1930s, but was supplanted by the new antibiotics and surgical techniques during World War II
In 2004, FDA allowed the production and marketing of the Phaenicia sericata larvae
In 2006, approx 50,000 treatments were applied to wounds using maggots
Low cost, simple, safe, ideal when surgical debridement is not the optimal choice
REPEATED DEBRIDEMENT - ENZYMATIC DEBRIDEMENT
Involves application of a cream or ointment to the wound. The action of the chemicals or enzymes contained in the cream work to loosen the dead tissue, which is then manually removed Fast acting
Minimal or no damage to healthy tissue with proper application.
May be used as the primary technique for debridement in some cases when surgical debridement is not feasible owing to bleeding disorders or patient is not fit for surgery
Combined therapy, such as initial surgical debridement followed by serial debridement using an enzymatic agent is effective for many patients with chronic, indolent, or nonhealing wounds
POST- DEBRIDEMENT SOFT TISSUE COVER
Presence of large soft tissue defect after surgical debridement often makes primary closure difficult
When possible, the least invasive methods of coverage are employed
eg. Delayed primary closure
Vacuum assisted closure
However, many wounds are not amenable to delayed primary closure and require plastic surgical techniques
- Split Skin Graft
- Local and Pedicle Flaps
- Free Flaps
VACUUM ASSISTED CLOSURE
Using a vacuum source to draw fluid out of the wound to accelerate debridement and promote healing
Not for acutely ischaemic foot, tumour wound
Special precaution : patient on anticoagulant
Wound bed preparation prior to initiation of treatment
Optimal level of negative pressure ~125mmHg
Most effective if applied in a cyclical pattern 5 mins on, 2 mins off
Advantage : - cheap - Ideal for difficult- to heal wounds Disadvantages : - restricts patient mobility
DIABETIC FOOT INFECTIONS -- CELLULITIS
9 times more frequent in diabetic compare to nondiabetic patients
Infection is confined to the dermal and subcutaneous layers
Commonly caused by Group A Streps & Staph
Entry : skin cracks, fissures, blister, insect bites
Antibiotics
DIABETIC FOOT INFECTIONS - OSTEOMYELITIS A difficult problem to treat & heal
The combined effects of peripheral vascular disease, neuropathy, and repetitive trauma produce complex lesions with exposed bone, surrounding cellulitis, and soft tissue gangrene
Plain x-rays, gallium scan, MRI
Bone culture
DIABETIC FOOT INFECTIONS - OSTEOMYELITIS
Diabetes Care August 2006 vol. 29 no. 8 1727-1732
A Clinico-microbiological Study of Diabetic Foot Ulcers in an Indian
Tertiary Care Hospital Ravisekhar Gadepalli, MSC; Benu Dhawan, MD; Vishnubhatla Sreenivas, PHD; Arti Kapil, MD1; A.C. Ammini, MD; Rama Chaudhry, MD
All patients had Wagner 3-5 ulcers 62.5% had associated osteomyelitis
DIABETIC FOOT INFECTION - OSTEOMYELITIS
If osteomyelitis is confirmed from initial deep cultures or histopathology, further aggressive resection of all affected bone is warranted
DEBRIDE ALL DEAD BONE & SOFT TISSUE till viable, bleeding bone & soft tissue
Staph aureus penetrates and survives in bone cells
* BONE PENETRATION OF ANTIBIOTICS * Fluoroquinolones ( ciprofloxacin, ofloxacin, moxifloxacin), Fucidic acid
NECROTISING FASCIITIS IN DIABETIC
Incidence on the rise
70% of patients are diabetic
MEDICAL & SURGICAL EMERGENCY !
Highly fatal ( overall morbidity & mortality : 70-80% )
Group A hemolytic streptococci ( Strep pyogenes ) and
Staph aureus, alone or in synergism, are frequently the initiating infecting bacteria
However, other aerobic and anaerobic pathogens may be present, including Bacteroides, Clostridium, Peptostreptococcus, Enterobacteriaceae, coliforms, Proteus, Pseudomonas, and Klebsiella.
Poor prognostic factors : advanced age, poor glycaemic control, long duration of diabetes & delayed referral
NECROTISING FASCIITIS
Progressive, rapidly spreading infection along the deep fascia plane & extensive necrosis of the subcutaneous tissues & muscle without a corresponding necrosis of the overlying skin until much later
Early features : Fever, pain, tachycardia, swelling, induration, cellulitis
Late features : Severe pain & tenderness disproportionate to skin changes, skin discolouration ( purplish black ), blister or bullae, crepitus, septicaemic shock, multiorgan failure
X-rays : subcutaneous gas
Antibiotics
Extensive surgical debridement & fasciotomy : delay for 24 hours mortality
THE ISCHAEMIC DIABETIC FOOT
UNLESS THERE IS ADEQUATE REPERFUSION OF THE FOOT / LEG, ANTIBIOTICS TREATMENT
AND SURGERY WILL FAIL & AMPUTATION WILL BE NEEDED
SURGERY IN THE DIABETIC FOOT
Historically, diabetic foot surgery was largely done in the presence of acute infection or when in need of amputation
With better understanding of the pathophysiology of diabetic foot disease, we have began to recognize the importance of elective diabetic foot surgery in helping patients to stay active and ulcer free
CLASSIFICATION OF SURGERY IN THE DIABETIC FOOT
CLASS PURPOSE EXAMPLES I ( Elective ) For painful deformities in patients Realignment osteotomies, without neuropathy or open wounds tendon balancing procedures, II ( Prophylactic ) For prevention of ulceration in patients arthrodeses & Charcot with neuropathy but no open wounds reconstructions III ( Curative ) To assist healing of ulcers in patients Partial or complete removal of with neuropathy bone such as metatarsal head, sesamoid, accessory bone, exostosis, calcanectomy, soft tissue cover / reconstructions IV ( Emergent / To arrest / limit progression of acute Amputations, debridements, Ablative ) infection, eliminate infected and incision and drainage necrotic tissue Armstrong DG, Lavery LA, Frykberg RG. Validation of a diabetic foot surgery classification. Int Wound J 2006;3(3): 240-246
ELECTIVE & PROPHYLACTIC SURGERY FOR THE DIABETIC FOOT
GOALS :
1) Stability
2) Realignment
3) Platigrade foot amendable to bracing or accomodation
4) Reduction of pressure points / surgical offloading
ELECTIVE / PROPHYLACTIC SURGERY
FOREFOOT :
HALLUX and FIRST METATARSALPHALANGEAL JOINT : - SESAMOIDECTOMY / EXOSTECTOMY
- HALLUX INTERPHALANGEAL ARTHROPLASTY / ARTHRODESIS
- RESECTION OF FIRST METATARSAL HEAD
- OSTEOTOMIES OF THE PHALANX AND FIRST METATARSAL LESSER DIGITS : - LESSER METATARSAL OSTEOTOMIES : Shortening osteotomy Elevating osteotomy - LESSER METATARSAL HEAD RESECTION
ELECTIVE / PROPHYLACTIC SURGERY
MIDFOOT :
- EXOSTECTOMY
- REALIGNMENT MIDFOOT OSTEOTOMIES + ARTHRODESIS
- single plane vs multiplane
REARFOOT : - TRIPLE ARTHRODESIS
- REALIGNMENT CALCANEAL OSTEOTOMIES
- TALECTOMY + TIBIAL-CALCANEAL ARTHRODESIS
- CALCANECTOMY ( partial / total )
OPTIMIZE THE HOST Correct and reverse all correctable negative factors on wound healing : - Anemia - Diabetes - Heart Failure - Malnutrition - Smoking - Steroid - Vitamin deficiency - Uraemia
FORMULATE A WOUND CARE PLAN Optimal wound care is crucial for healing but it is not the only way to treat the diabetic foot ulcer
Infection complicates treatment of a diabetic foot ulcer, making a more aggressive wound care strategy necessary
One particular dressing should not be used for all stages of wound
A long process time, patience, perseverence -- Dedicated team of doctors and nurses Problems to be addressed in DFU : -- Exudate, bacterial load, slough, granulation
CHOOSING THE APPROPRIATE DRESSING
INFECTED : surgical debridement + silver dressing
EXUDATIVE : absorptive dressing
eg. Hydrofibres, Alginates,
Composite dressings,
Foam dressings
SLOUGHY : surgical / enzymatic /
maggot debridement
DRY : Hydrogels
SAVING EVERY LEG ? Reducing the number of lower extremity
amputations is a goal for all doctors caring for patients with diabetes
However, the numbers of limb-threatening infections continue to rise each year
Failures in limb salvage attempts do occur
These failures result in multiple trips to the operating room, significant potential morbidity and prolonged disability
AMPUTATION
Somewhere in the world, a leg is lost to diabetes every 30 seconds
Diabetics are 40x more likely to undergo amputation of the leg than non-diabetics
>85 % of amputation begins with a foot ulcer
Those who undergo a lower limb amputation have up to 30% chance of undergoing similar amputation on the contralateral limb within 3 years and up to 50% chance in 5 years
Mortality rate post amputation: 11-41% after 1 year 20-50% after 3 years 39-68% after 5 years
Two goals : ABLATION + RECONSTRUCTION
refashioned the viable residual limb so that an appropriate prosthesis may be fitted to assist functional mobility
AMPUTATION
STRAUSS WOUND GRADING SCORE
VARIABLES 2 1.5 1 0.5 0
PERFUSION
DEPTH
SIZE
INFECTION
WOUNDBASE
Warm
Skin & sub-Q
< thumb
Clean & contam.
Red
Cool
Musc & tendons
Thumb fist
Cellulitis
Yellow-white
Cold
Bone & Joint
>fist
Septic
Black
=8 0% amputation
MINOR AMPUTATIONS :
- Disarticulation
- Ray amputation
- Midfoot amputation
- Syme amputation
MAJOR AMPUTATIONS :
- Below knee amputation
- Above knee amputation
- Hip disarticulation
ENERGY CONSUMPTION AND AMPUTATION LEVEL
AMPUTATION LEVEL % ENERGY BEYOND
BASELINE
Long BKA 10
Medium BKA 25
Short BKA 40
Bilateral medium BKA
41
Average AKA 65
Miller; Orthopaedic Review: Pg. 218.
AFTER AMPUTATION .
Specialty diabetic foot clinic : recurrence rate 25-80%/year
Self-monitoring
- to identify signs of disease and precursors to injury
- many diabetic patients with a high risk for ulceration cannot see
their feet ! ( obesity, limited joint mobility, visual impairment )
- by the time patients in this study were able to visualize areas of
concern, it was too late, and an ulceration had already developed
Self-care
CHALLENGE : PREVENTING RECURRENCE
CHALLENGE - PATIENTS
EDUCATION & SUPPORT
PERCEPTION & BEHAVIORAL
CHANGE
Overcoming : - Ignorance / Misconception - Fear - Denial - Uncooperativeness - Social problems
Increase awareness of :
- DM & its many consequences - Methods of care & support available
CHALLENGE THE OLD DIABETIC PATIENTS DIFFERENT FROM THE YOUNGER PATIENTS : Poorer limb perfusion
Poorer healing / tissue regeneration
Weaker immune defence
Comorbidities ++
Soft tissue fragility / osteoporosis
Poor nutrition
Poor vision / memory / senility
Limited mobility
Social and financial support problems
Dependant, poor self care, neglect
NURSING HOME PROBLEMS
Two-thirds of elderly patients undergoing amputation do not return to independent life
CHALLENGE HEALTHCARE PERSONNEL
Organisation : WOUND CARE TEAM - 70% of wound dressings are applied by the bedside
nurse, NOT the wound care specialists
Training ( Knowledge & Skills ) :
- Train more people
- Keep in touch with the latest development - Learn what to do, what not to do, how to do it
Early detection & referral :
- Educate & build a positive working relationaship with primary health care
providers
Budget & allocation
CHALLENGE HEALTH CARE SYSTEM
Although there have been many advances in the management of
the diabetic foot, it remained a major global public health
problem
Where have we failed ?
Health Care Policy ?
Health Care Budgeting ?
Health Care Organisation ?
Policy Implementation ?
What needs to be done ? Present ? Future ?
What about the poorer countries and their people ?
CHALLENGE - RESEARCH
FROM THE BENCH TO THE BEDSIDE - integration of resources into a
coordinated effort and monitoring
pathway to bring products of research
and technology to the patients
FUTURE OF DIABETIC WOUND CARE
Narrowing gap between basic science and clinical application
Necessary to understand the complex interactions of various physiologic components in wound healing
SMART BIOACTIVE DRESSING -- that responds to the needs of the wound by releasing factors needed for healing
STEM CELLS as a potentiator of healing by
replacing or activating senescent cells in the wound eg. Bioengineered skin
OVERALL MANAGEMENT
PREVENTION ! PREVENTION ! PREVENTION !
Early detection and intervention
Medical management of diabetes and comorbid conditions
Targeted antibiotic coverage of infection
TEAM EFFORT
Wound care and dressing, off-loading / pressure relief
Adjuvant therapies (eg. Hyperbaric O2 ) & Nutrition
Post-op follow-up, podiatric care / foot wear and orthoses
PREVENT RECURRENCE !
Doctor treating a foot ulcer : 17th Century, after David Teniers the younger
THANK YOU